Disorders muscular dystrophy association muscular atrophy spinal. Medical search. Frequent questions

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Anatomy35

Spinal Cord Muscle, Skeletal Motor Neurons Anterior Horn Cells Muscles Muscle Fibers, Skeletal Chromosomes, Human, Pair 5 Sarcolemma Myoblasts Spinal Nerve Roots X Chromosome Chromosomes, Human, Pair 4 Spinal Nerves Coiled Bodies Spinal Canal Neuromuscular Junction Brain Diaphragm Cells, Cultured Axons Fibroblasts Intranuclear Inclusion Bodies Spine Cell Line Satellite Cells, Skeletal Muscle Inclusion Bodies Neurons Sural Nerve Ganglia, Spinal Myoblasts, Skeletal Muscle Cells Cell Nucleus Fundus Oculi HeLa Cells Thoracic Vertebrae

Organisms8

Mice, Inbred mdx Mice, Transgenic Mice, Inbred C57BL Mice, Knockout Dependovirus Mice, Mutant Strains Zebrafish Animals, Newborn

Diseases68

Muscular Dystrophies Muscular Atrophy, Spinal Muscular Dystrophy, Duchenne Spinal Muscular Atrophies of Childhood Muscular Dystrophy, Animal Atrophy Muscular Atrophy Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Emery-Dreifuss Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Corneal Dystrophies, Hereditary Spinal Cord Injuries Muscular Dystrophy, Oculopharyngeal Disease Models, Animal Fuchs' Endothelial Dystrophy Spinal Cord Diseases Neuromuscular Diseases Retinal Dystrophies Optic Atrophy Motor Neuron Disease Muscular Diseases Muscle Weakness Multiple System Atrophy Contracture Spinal Cord Neoplasms Neuroaxonal Dystrophies Spinal Diseases Syndrome Spinal Cord Compression Spinal Neoplasms Walker-Warburg Syndrome Sarcoglycanopathies Cardiomyopathies Nerve Degeneration Bulbar Palsy, Progressive Spinal Stenosis Charcot-Marie-Tooth Disease Scoliosis Disease Progression Olivopontocerebellar Atrophies Reflex Sympathetic Dystrophy Arthrogryposis Vocal Cord Paralysis Myositis Spinal Injuries Amyotrophic Lateral Sclerosis Vitelliform Macular Dystrophy Gyrate Atrophy Neuromuscular Junction Diseases Nervous System Diseases Spinal Curvatures Spinal Cord Ischemia Retinal Degeneration Intellectual Disability Geographic Atrophy Myotonic Disorders Cardiomyopathy, Dilated Neurodegenerative Diseases Paraplegia Myoclonic Epilepsies, Progressive Distal Myopathies Retinitis Pigmentosa Fasciculation Substance-Related Disorders Ophthalmoplegia

Chemicals and Drugs48

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Dystrophin Sarcoglycans Dystroglycans Neuronal Apoptosis-Inhibitory Protein Utrophin Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Nerve Tissue Proteins Thymopoietins Collagen Type VI Ribonucleoproteins, Small Nuclear Muscle Proteins DEAD Box Protein 20 Dystrophin-Associated Proteins Creatine Kinase Lamin Type A Laminin Dystrophin-Associated Protein Complex Caveolin 3 Poly(A)-Binding Protein II Receptors, Androgen snRNP Core Proteins Cytoskeletal Proteins Calpain RNA, Messenger Membrane Proteins Plectin Genetic Markers Myostatin Connectin Glycine-tRNA Ligase Oligonucleotides, Antisense DNA DNA Primers Lamins Creatine Kinase, MM Form Nuclear Proteins Membrane Glycoproteins Codon, Nonsense Morpholinos Mannosyltransferases N-Acetylglucosaminyltransferases Peptides Poly(A)-Binding Protein I Valproic Acid

Analytical, Diagnostic and Therapeutic Techniques and Equipment30

Pedigree Disease Models, Animal Heterozygote Detection Injections, Spinal Genetic Therapy Electromyography Magnetic Resonance Imaging DNA Mutational Analysis Anesthesia, Spinal Chromosome Mapping Muscle Strength Prenatal Diagnosis Spinal Fusion Immunohistochemistry Genetic Testing Polymerase Chain Reaction Blotting, Western Severity of Illness Index Biopsy Reverse Transcriptase Polymerase Chain Reaction Electroretinography Fluorescent Antibody Technique Muscle Denervation Treatment Outcome Myelography Stem Cell Transplantation Analysis of Variance Models, Biological Gene Transfer Techniques Reproducibility of Results

Psychiatry and Psychology17

Bipolar Disorder Mental Disorders Anxiety Disorders Mood Disorders Motor Activity Depressive Disorder, Major Attention Deficit Disorder with Hyperactivity Depressive Disorder Cognition Disorders Intellectual Disability Obsessive-Compulsive Disorder Stress Disorders, Post-Traumatic Autistic Disorder Phobic Disorders Child Development Disorders, Pervasive Psychotic Disorders Substance-Related Disorders

Phenomena and Processes47

Exons Mutation Phenotype Chromosomes, Human, Pair 5 Genetic Linkage Genes, Recessive X Chromosome Chromosomes, Human, Pair 4 Homozygote Genes, Dominant Trinucleotide Repeat Expansion Gene Deletion Heterozygote Muscle Strength Mutation, Missense Base Sequence RNA Splicing Consanguinity Gene Expression Regulation Regeneration Time Factors Alternative Splicing Muscle Development Genetic Markers Genotype Amino Acid Sequence Neural Conduction Motor Activity Founder Effect Alleles Sequence Deletion Gene Expression Gene Dosage Transgenes Haplotypes Point Mutation Polymorphism, Single-Stranded Conformational Trinucleotide Repeats Lod Score Introns Glycosylation Genetic Vectors Frameshift Mutation Codon, Nonsense Protein Binding Cell Differentiation Muscle Contraction

Disciplines and Occupations3

Immunohistochemistry Genetic Counseling Chemistry, Analytic

Information Science4

Molecular Sequence Data Base Sequence Diagnostic and Statistical Manual of Mental Disorders Amino Acid Sequence

Named Groups1

Infant, Newborn

Health Care9

Genetic Counseling Genetic Testing Age of Onset Severity of Illness Index Family Health Age Factors Treatment Outcome Analysis of Variance Reproducibility of Results

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Information Science Health Care

Muscular Dystrophies Muscular Atrophy, Spinal Muscular Dystrophy, Duchenne Spinal Muscular Atrophies of Childhood Muscular Dystrophy, Animal Survival of Motor Neuron 1 Protein Atrophy SMN Complex Proteins Muscular Atrophy Survival of Motor Neuron 2 Protein Dystrophin Spinal Cord Myotonic Dystrophy Muscular Dystrophies, Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Mice, Inbred mdx Muscular Dystrophy, Emery-Dreifuss Sarcoglycans Muscular Disorders, Atrophic Muscle, Skeletal Bulbo-Spinal Atrophy, X-Linked Corneal Dystrophies, Hereditary Spinal Cord Injuries Dystroglycans Muscular Dystrophy, Oculopharyngeal Neuronal Apoptosis-Inhibitory Protein Utrophin Cyclic AMP Response Element-Binding Protein Motor Neurons Anterior Horn Cells Pedigree RNA-Binding Proteins Exons Disease Models, Animal Nerve Tissue Proteins Heterozygote Detection Fuchs' Endothelial Dystrophy Spinal Cord Diseases Mutation Thymopoietins Phenotype Neuromuscular Diseases Retinal Dystrophies Collagen Type VI Muscles Muscle Fibers, Skeletal Optic Atrophy Motor Neuron Disease Chromosomes, Human, Pair 5 Ribonucleoproteins, Small Nuclear Muscle Proteins Genetic Linkage Muscular Diseases Muscle Weakness Genes, Recessive Bipolar Disorder Mice, Transgenic DEAD Box Protein 20 Sarcolemma Dystrophin-Associated Proteins Creatine Kinase Myoblasts Spinal Nerve Roots Injections, Spinal X Chromosome Chromosomes, Human, Pair 4 Homozygote Lamin Type A Mental Disorders Genes, Dominant Spinal Nerves Laminin Trinucleotide Repeat Expansion Genetic Therapy Multiple System Atrophy Dystrophin-Associated Protein Complex Molecular Sequence Data Caveolin 3 Gene Deletion Electromyography Coiled Bodies Magnetic Resonance Imaging Poly(A)-Binding Protein II Contracture DNA Mutational Analysis Anesthesia, Spinal Anxiety Disorders Mood Disorders Receptors, Androgen Heterozygote snRNP Core Proteins Chromosome Mapping Muscle Strength Mice, Inbred C57BL Mutation, Missense Spinal Cord Neoplasms Base Sequence Spinal Canal Neuroaxonal Dystrophies Spinal Diseases

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